ClinVar Miner

List of variants in gene TRPV4 reported as uncertain significance by Genome Diagnostics Laboratory, Amsterdam University Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_021625.5(TRPV4):c.1139C>T (p.Thr380Met)	rs764949536	0.00006
NM_021625.5(TRPV4):c.958C>T (p.Arg320Ter)	rs142902080	0.00006

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